Simonelli F - Search Results

1

Care Pathway of RPE65-Related Inherited Retinal Disorders from Early Symptoms to Genetic Counseling: A Multicenter Narrative Medicine Project in Italy.

Simonelli F, Sodi A, Falsini B, Bacci G, Iarossi G, Di Iorio V, Giorgio D, Placidi G, Andrao A, Reale L, Fiorencis A, Aoun M. Simonelli F, et al. Clin Ophthalmol. 2021 Dec 2;15:4591-4605. doi: 10.2147/OPTH.S331218. eCollection 2021. Clin Ophthalmol. 2021. PMID: 34880596 Free PMC article.

2

Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene.

Testa F, Ziviello C, Rinaldi M, Rossi S, Di Iorio V, Interlandi E, Ciccodicola A, Banfi S, Simonelli F. Testa F, et al. Among authors: simonelli f. Eur J Ophthalmol. 2006 Sep-Oct;16(5):779-81. doi: 10.1177/112067210601600524. Eur J Ophthalmol. 2006. PMID: 17061239

3

A novel mutation in the VMD2 gene in an Italian family with Best maculopathy.

Sodi A, Passerini I, Simonelli F, Testa F, Menchini U, Torricelli F. Sodi A, et al. Among authors: simonelli f. J Fr Ophtalmol. 2007 Jun;30(6):616-20. doi: 10.1016/s0181-5512(07)89667-7. J Fr Ophtalmol. 2007. PMID: 17646752

4

A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene.

Testa F, Rossi S, Passerini I, Sodi A, Di Iorio V, Interlandi E, Della Corte M, Menchini U, Rinaldi E, Torricelli F, Simonelli F. Testa F, et al. Among authors: simonelli f. Br J Ophthalmol. 2008 Nov;92(11):1467-70. doi: 10.1136/bjo.2008.143776. Epub 2008 Aug 14. Br J Ophthalmol. 2008. PMID: 18703557

5

Evaluation of Italian patients with leber congenital amaurosis due to AIPL1 mutations highlights the potential applicability of gene therapy.

Testa F, Surace EM, Rossi S, Marrocco E, Gargiulo A, Di Iorio V, Ziviello C, Nesti A, Fecarotta S, Bacci ML, Giunti M, Della Corte M, Banfi S, Auricchio A, Simonelli F. Testa F, et al. Among authors: simonelli f. Invest Ophthalmol Vis Sci. 2011 Jul 29;52(8):5618-24. doi: 10.1167/iovs.10-6543. Invest Ophthalmol Vis Sci. 2011. PMID: 21474771

6

The role of optical coherence tomography in an atypical case of oculocutaneous albinism: a case report.

Rossi S, Testa F, Gargiulo A, Di Iorio V, Pierri RB, D'Alterio FM, Corte MD, Surace E, Simonelli F. Rossi S, et al. Among authors: simonelli f. Case Rep Ophthalmol. 2012 Jan;3(1):113-7. doi: 10.1159/000337489. Epub 2012 Mar 27. Case Rep Ophthalmol. 2012. PMID: 22548044 Free PMC article.

7

Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy.

Testa F, Rossi S, Sodi A, Passerini I, Di Iorio V, Della Corte M, Banfi S, Surace EM, Menchini U, Auricchio A, Simonelli F. Testa F, et al. Among authors: simonelli f. Invest Ophthalmol Vis Sci. 2012 Jul 3;53(8):4409-15. doi: 10.1167/iovs.11-8201. Invest Ophthalmol Vis Sci. 2012. PMID: 22661472 Free PMC article.

8

Macular abnormalities in Italian patients with retinitis pigmentosa.

Testa F, Rossi S, Colucci R, Gallo B, Di Iorio V, della Corte M, Azzolini C, Melillo P, Simonelli F. Testa F, et al. Among authors: simonelli f. Br J Ophthalmol. 2014 Jul;98(7):946-50. doi: 10.1136/bjophthalmol-2013-304082. Epub 2014 Feb 13. Br J Ophthalmol. 2014. PMID: 24532797 Free PMC article.

9

Macular function and morphologic features in juvenile stargardt disease: longitudinal study.

Testa F, Melillo P, Di Iorio V, Orrico A, Attanasio M, Rossi S, Simonelli F. Testa F, et al. Among authors: simonelli f. Ophthalmology. 2014 Dec;121(12):2399-405. doi: 10.1016/j.ophtha.2014.06.032. Epub 2014 Aug 2. Ophthalmology. 2014. PMID: 25097154 Free PMC article.

10

Standard versus trans-epithelial collagen cross-linking in keratoconus patients suitable for standard collagen cross-linking.

Rossi S, Orrico A, Santamaria C, Romano V, De Rosa L, Simonelli F, De Rosa G. Rossi S, et al. Among authors: simonelli f. Clin Ophthalmol. 2015 Mar 18;9:503-9. doi: 10.2147/OPTH.S73991. eCollection 2015. Clin Ophthalmol. 2015. PMID: 25834386 Free PMC article.

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